rs3737296
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs3737296(A;A) |
| Make rs3737296(A;G) |
| Make rs3737296(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 220652181 |
| Gene | MARK1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3737296 |
| dbSNP (classic) | rs3737296 |
| ClinGen | rs3737296 |
| ebi | rs3737296 |
| HLI | rs3737296 |
| Exac | rs3737296 |
| Gnomad | rs3737296 |
| Varsome | rs3737296 |
| LitVar | rs3737296 |
| Map | rs3737296 |
| PheGenI | rs3737296 |
| Biobank | rs3737296 |
| 1000 genomes | rs3737296 |
| hgdp | rs3737296 |
| ensembl | rs3737296 |
| geneview | rs3737296 |
| scholar | rs3737296 |
| rs3737296 | |
| pharmgkb | rs3737296 |
| gwascentral | rs3737296 |
| openSNP | rs3737296 |
| 23andMe | rs3737296 |
| SNPshot | rs3737296 |
| SNPdbe | rs3737296 |
| MSV3d | rs3737296 |
| GWAS Ctlg | rs3737296 |
| GMAF | 0.2429 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 18492799] Haplotype rs12740310*C-rs3737296*G-rs12410279*A was overtransmitted (p(corrected)=0.0016), with a relative risk for autism of 1.8 in homozygous carriers
